U.S. patent application number 09/829651 was filed with the patent office on 2002-10-10 for liquid sample dispensing methods for precisely delivering liquids without crossover.
Invention is credited to Devlin, William Jackson SR..
Application Number | 20020144747 09/829651 |
Document ID | / |
Family ID | 25255134 |
Filed Date | 2002-10-10 |
United States Patent
Application |
20020144747 |
Kind Code |
A1 |
Devlin, William Jackson
SR. |
October 10, 2002 |
LIQUID SAMPLE DISPENSING METHODS FOR PRECISELY DELIVERING LIQUIDS
WITHOUT CROSSOVER
Abstract
A method for reducing carryover of and delivering liquid taken
from a source container by a dispensing means to a target container
by spinning the target container so that any liquid within the
target container is removed from the dispensing means prior to
dispensing liquid into the target container.
Inventors: |
Devlin, William Jackson SR.;
(Lincoln University, PA) |
Correspondence
Address: |
Dade Behring Inc.
Legal Dept. - Patents
Attn: Lois K. Ruszala
1717 Deerfield, Rd., #778
Deerfield
IL
60015-0778
US
|
Family ID: |
25255134 |
Appl. No.: |
09/829651 |
Filed: |
April 10, 2001 |
Current U.S.
Class: |
141/129 |
Current CPC
Class: |
G01N 2035/1034 20130101;
Y10T 436/11 20150115; B01L 3/0293 20130101; B01L 9/00 20130101;
G01N 35/1016 20130101; Y10T 436/2575 20150115 |
Class at
Publication: |
141/129 |
International
Class: |
B67C 003/00 |
Claims
What is claimed is:
1. A method for reducing carryover of first target vessel liquid
contained in a first target vessel and a sampling pipette
containing source liquid, the method comprising: spinning the first
target vessel so that first target vessel liquid contained therein
is displaced away from the central portion of the target vessel;
forming a first droplet of source liquid at the nozzle of the
sampling pipette; lowering the sampling pipette into the central
portion of the target vessel a distance sufficient to cause the
first droplet of source liquid to contact the bottom of the first
target vessel without the sampling pipette or the droplet touching
first target vessel liquid disposed therein, so that the first
droplet of source liquid is spun off from the sampling pipette into
the target vessel.
2. The method of claim 1 further comprising: spinning a second
target vessel so that second target vessel liquid contained therein
is displaced away from the central portion of the second target
vessel; forming a second droplet of source liquid at the nozzle of
the sampling pipette; lowering the sampling pipette into the
central portion of the second target vessel a distance sufficient
to cause the second droplet of source liquid to contact the bottom
of the second target vessel without the sampling pipette or the
droplet touching second target vessel liquid disposed therein, so
that the second droplet of source liquid is spun off from the
sampling pipette into the second target vessel.
3. The method of claim 1 wherein the target vessel is axially
symetrical.
4. The method of claim 1 wherein the sampling pipette is either a
permanent or disposable sampling pipette.
5. A method for reducing carryover of first target vessel liquid
contained in a first target vessel and a sampling pipette
containing source liquid, the method comprising: inclining the
first target vessel so that first target vessel liquid contained
therein is displaced away from the central portion of the target
vessel; forming a first droplet of source liquid at the nozzle of
the sampling pipette; lowering the sampling pipette into the
central portion of the target vessel a distance sufficient to cause
the first droplet of source liquid to contact the bottom of the
first target vessel without the sampling pipette or the droplet
touching first target vessel liquid disposed therein, so that the
first droplet of source liquid is spun off from the sampling
pipette into the target vessel.
6. The method of claim 5 further comprising: inclining a second
target vessel so that second target vessel liquid contained therein
is displaced away from the central portion of the second target
vessel; forming a second droplet of source liquid at the nozzle of
the sampling pipette; lowering the sampling pipette into the
central portion of the second target vessel a distance sufficient
to cause the second droplet of source liquid to contact the bottom
of the second target vessel without the sampling pipette or the
droplet touching second target vessel liquid disposed therein, so
that the second droplet of source liquid is spun from the sampling
pipette into the target vessel.
7. The method of claim 5 wherein the target vessel is axially
symetrical.
8. The method of claim 5 wherein the sampling pipette is either a
permanent or disposable sampling pipette.
9. A method for delivering an amount of liquid from a source vessel
into a target vessel, the method comprising: aspirating a known
volume of liquid from the source container into an aspirating
probe; dispensing a major portion of the volume of liquid into the
target vessel while the target vessel is stationary, at the same
time leaving a minor portion of liquid within the aspirating probe;
spinning the target vessel so that the major portion of liquid
contained therein is displaced away from the central portion of the
target vessel; forming a droplet of the minor portion of source
liquid at the nozzle of the sampling pipette; lowering the sampling
pipette into the central portion of the target vessel a distance
sufficient to cause the droplet of source liquid to contact the
bottom of the target vessel without the droplet touching liquid
disposed therein, so that the droplet of source liquid is spun off
from the sampling pipette into the target vessel.
10. The method of claim 9 wherein the target vessel is axially
symetrical.
11. The method of claim 9 wherein the sampling pipette is either a
permanent or disposable sampling pipette.
12. A method for delivering an amount of source liquid from a
source vessel into a target vessel containing target liquid
therein, the method comprising: aspirating a known volume of source
liquid from the source container into an aspirating probe; spinning
the target vessel so that target liquid contained therein is
displaced away from the central portion of the target vessel;
lowering the sampling pipette into the central portion of the
target vessel a distance sufficient to cause a major portion of the
volume of source liquid to contact the bottom of the target vessel
without the major portion touching target liquid disposed therein,
so that the major portion of source liquid is spun off from the
sampling pipette into the target vessel; continuing to spin the
target vessel so that all liquid contained therein is displaced
away from the central portion of the target vessel; forming a
droplet of the remaining droplet portion of source liquid at the
nozzle of the sampling pipette; lowering the sampling pipette into
the central portion of the target vessel a distance sufficient to
cause the remaining droplet portion of source liquid to contact the
bottom of the target vessel without the remaining droplet portion
touching liquid disposed therein, so that the remaining droplet
portion of source liquid is spun off from the sampling pipette into
the target vessel.
13. The method of claim 13 wherein the target vessel is axially
symmetrical.
14. The method of claim 13 wherein the sampling pipette is either a
permanent or disposable sampling pipette.
Description
FIELD OF THE INVENTION
[0001] The present invention relates to liquid sample dispensing in
which a sampling pipette aspirates liquids from a sample or reagent
container and dispenses the aspirated liquid into a reaction
vessel. More particularly, the invention relates to a system for
precisely delivering an amount of liquid from a sample or reagent
container into a reaction tube and for reducing carry-over of
liquid from one reaction tube to the next, thereby protecting the
integrity of the solution within the reaction tube.
BACKGROUND OF THE INVENTION
[0002] Various types of tests related to patient diagnosis and
therapy can be performed by analysis of a sample of a patient's
infections, bodily fluids or abscesses. Such samples are typically
placed in sample vials, extracted from the vials, combined with
various reagents in special reaction vessels or tubes, incubated,
and analyzed to aid in treatment of the patient. Automated clinical
analyzers adapted to perform these operations typically handle
liquids by aspiration and pressurized dispensing from the sample
vials into a reaction vessel using a sampling probe or pipette. In
general, a sampling pipette is immersed into a liquid held in a
suitable container. A partial vacuum is produced in the pipette in
an amount sufficient to draw the required amount of liquid up into
the pipette through its nozzle, and the pipette is taken to a
station holding a pre-treatment or reaction vessel. At that
station, pressure is applied to the interior of the pipette in an
amount sufficient to dispense the desired amount of liquid out of
the nozzle. The clinical analyzer typically uses a portion or
aliquot of the patient's sample that is aspirated from the vial by
a sampling pipette. The entire aspirated aliquot or a portion
thereof may then be dispensed from the sampling pipette into a
reaction vessel or into a sample pre-treatment vessel from which
treated sample is later aspirated. Automated clinical analyzers
also typically include reagent pipettes adapted to aspirate reagent
from reagent containers and to dispense the entire aspirated
reagent or a portion thereof into the sample pre-treatment vessel
or directly into the reaction vessel.
[0003] Conventional pipettes suffer the disadvantage that liquid
tends to remain on the exterior surface of the pipette when the
pipette is withdrawn after aspiration. In cases of small volumes of
aspirated liquid, any excess liquid carried on the exterior of the
pipette may be a significant volume with respect to or could even
exceed the volume of the aspirated liquid. Pipettes are designed to
accurately dispense a predicted volume of liquid; however, any
liquid on the exterior surface of the nozzle at the orifice might
also be dispensed. Alternatively, the presence of the liquid on the
exterior surface might cause the dispensed quantity of liquid to
perfuse up the exterior surface, rather than to move into a target
vessel. In either case, the volume of liquid received by the vessel
is altered in an unpredictable fashion.
[0004] Another disadvantage is that reusable probes used to deliver
liquid aliquots from successive containers such as tubes or liquid
reagent vessels are a source of intra-sample carryover or
contamination. Regardless of application, the sampling pipette and
reagent pipette must also be thoroughly cleaned and dried between
aspirations of different liquids to avoid carryover
contamination.
[0005] In the prior art are various solutions to the inter-related
carryover and contamination problems. To prevent
cross-contamination between samples, the pipette may be provided
with a removable and disposable "pipette tip" which is the sole
portion of the probe to contact the sample liquid. However,
disposable pipettes are costly and over a long period of time,
become an unexpectedly high item of unwanted expense. Some
analyzers include a wiping operation between each aspiration.
However, wiping is an extra potential source of contamination, and
also introduces additional automated mechanisms that lower the
throughput rate and increase the expense of an analyzer.
[0006] In order to minimize contamination and carry-over between
samples, the probe may be flushed or washed with a diluent liquid
such as water. It has also been proposed to utilize a separate
probe wash sleeve through which a pressurized rinse liquid is
flushed (U.S. Pat. No. 4,756,201). In general, a probe wash chamber
is utilized including a wash fluid input into the pipette and a
fluid output or exhaust for removing the fluid once the exterior of
the pipette has been cleaned. Wash chambers can leak fluid and also
can channel along only one side or a portion of the pipette which
can leave residue on the pipette exterior. Additionally, if a last
drop of wash diluent does not drop off the pipette and is carried
back to an aspiration vessel, the droplets dilute the sample or
reagent, introducing unwanted sources of error.
[0007] Another technique shown, for example in U.S. Pat. No.
3,266,322, aspirates air through the probe by means of a vacuum
pump or the aspirating pump used to withdraw the sample liquid from
the sample container. Such aspiration, however, introduces the
possibility of drawing the unwanted carry-over contaminants deeper
into the tubing and apparatus which comprises the sampling
system.
[0008] U.S. Pat. No.: 4,347,875 discloses a "self-cleaning" nozzle
for causing liquid remaining behind on the exterior surface of the
nozzle to automatically locate itself other than at the aspirating
and dispensing orifice. The nozzle comprises a liquid-confining
wall extending about a longitudinal axis and terminating in a
liquid-dispensing orifice, and an exterior surface having a portion
adjacent to the aperture that is adapted to be immersed into a
source of the liquid during aspiration. The wall attracts liquid
remaining on the adjacent exterior surface after aspiration to loci
spaced from the orifice a distance effective to prevent liquid
remaining on the exterior surface from interfering with the
dispensing of the liquid.
[0009] U.S. Pat. No. 4,871,682 discloses an air knife positioned to
direct a stream or blast of air across the tip of a sample probe as
it is withdrawn from a vessel containing a reagent, diluent, and
patient sample solution. After the probe is flushed with diluent,
the air knife drives any droplets of diluent fluid off the probe
tip into the vessel and thereby prevents contamination or dilution
of the sample material in the sample containers.
[0010] U.S. Pat. No. 5,506,142 discloses a wash probe in which the
simultaneous introduction of pressurized air and water creates a
turbulent flow including the use of a pressurized gas stream of
short duration to blow the residue of the previous sample out of
the probe prior to washing with additional diluent liquid. Also, a
waste receptacle is provided which uses a filtered air vent and a
liquid saturated material around the probe receiving opening to
prevent the escape of aerosols from the receptacle.
[0011] U. S. Pat. No. 5,506,142 provides for a probe wash in which
the simultaneous introduction of pressurized air and water creates
a turbulent flow including the use of a portion droplet of liquid
into contact with the bottom of the target container so that the
entire remaining smaller droplet is dispensed. Sensing to confirm
the "touching-off" of this smaller droplet assures that the total
volume of liquid dispensed in the two steps is bounded at a maximum
by the originally aspirated volume and at a minimum by the volume
of liquid dispensed in the first step alone.
[0012] Briefly summarized, the invention provides a method for
reducing carryover of and precisely delivering liquid from a source
container to first and subsequent target containers by spinning the
target containers so that any liquid within the target container is
removed from the dispensing means.
BRIEF DESCRIPTION OF THE DRAWINGS
[0013] For more complete understanding of the invention reference
is made to the embodiment illustrated in greater detail in the
accompanying drawings and the following detailed description.
[0014] FIG. 1 is a schematic diagram of an automated analyzer in
which the present invention may be used to advantage;
[0015] FIGS. 2-6 schematically illustrate the present invention for
reducing carryover of liquid from a source container to first and
subsequent target containers; and,
[0016] FIGS. 7-11 schematically illustrate an alternate embodiment
of the present invention for delivering liquid from a source
container to an empty target container.
[0017] FIGS. 12-17 schematically illustrate an embodiment of the
present invention for delivering liquid from a source container to
a target container already containing liquid.
DETAILED DESCRIPTION OF THE INVENTION
[0018] The method and apparatus of this invention will be described
initially with particular reference to FIG. 1 of the drawings. FIG.
1 shows schematically the elements of a conventional automatic
chemical analyzer 10 comprising a sample cup carousel 11 supporting
a plurality of open sample tubes 13, a test vessel carousel 14,
adapted to hold a plurality of test vessels 12 and to provide
plurality of reagent liquid cartridges 20, illustrated as disposed
beneath a cut out portion 21 of a lid 22, which covers various
thermally controlled compartments. The vessel carousel 14,
preferably in the form of a wheel, has about one hundred separate
open cavities 17 for holding vessels 12, the inner wall of each
cavity having an opening to allow transmission of light. Vessels 12
are seen in FIG. 2 as having a generally cylindrically shape around
a central axis 36, also having an open top 38 and a closed bottom
40. Test vessel carousel 14 is provided with means 34 for rotating
selected ones of the test vessels 12 around its central axis 36,
the rotating means 34 being located proximate selected open
cavities 17 holding test vessels 12. Reagent cartridges 20 may be,
for example, a multi-compartment container such as those sold under
the tradename FLEX.RTM. by Dade Behring Inc., Deerfield, Ill., and
having a number of different reagents within the multi-compartments
23. A sample liquid arm 24 and a wash resource 26 used to clean a
liquid sample aspirating probe 28 described hereinafter are located
proximate the sample cup carousel 11 and vessel carousel 14. Sample
liquid arm 24 supports sample aspirating probe 28 and is mounted
onto a rotatable shaft 27 so that movement of sample liquid arm 24
describes an arc intersecting the sample cup carousel 11, test
vessels 12, and wash resource 26. Sample aspirating probe 28 is
adapted, for example by cooperation with a peristaltic vacuum pump,
to aspirate or withdraw from sample tubes 13 all of or aliquot
portions of a patient's specimen and to dispense all of or aliquot
portions of a patient's specimen to be tested by analyzer 10.
[0019] In a similar manner, a liquid reagent aspirating probe 25 is
rotatably mounted above vessel carousel 16 and is adapted to draw
reagent liquid from an appropriate compartment 23 of reagent liquid
cartridge 20 in cooperation with a peristaltic pump vacuum source
and to deposit reagent liquid within a predetermined vessel 12 for
processing by the chemical analyzer 10. Probe 25 optionally
comprises an ultrasonic mechanism used for aspirating, dispensing
and mixing reagents similar to that used in the DIMENSION.RTM.
chemical analyzer. Photometic analyzing means, not shown, located
beneath the vessel carousel 16 measures light absorbence through
the vessels 12 at various wavelengths, from which the presence of
analyte in the sample liquid may be determined. Photometic
analyzing means, not shown, located beneath the vessel carousel 16
measures light absorbence through the vessel 12 at various
wavelengths. The photometric analyzing means is of conventional
design and includes a photometer and a source lamp that emits a
light beam which passes through various lens housed in a rotatable
detector arm to a photodetector which, being mounted on the
outer-end of the detector arm adjacent the outer periphery of the
vessels 12, rotates about the vessel carousel 16. The photodetector
relays absorbence readings through the computer where the readings
are converted into concentration units. A conventional computer 18
using a microprocessor is used to control the various components of
the analyzer 10 and to store system parameter changes and test
results. The chemical analyzer 10 may be, for example, the
DIMENSION.RTM. clinical analyzer sold by Dade Behring Inc.,
Deerfield, Ill., or another similar analyzer commercially available
to clinical laboratories.
[0020] The present invention adds to analyzer 10 or similar
analyzers available to clinical laboratories a method to precisely
deliver an amount of liquid from a first sample tube 13 into a test
vessel 12 and for reducing carryover of liquid within a first test
vessel 12 tube to either a second test vessel 12 or to a second
sample tube 13, thereby protecting the integrity of the solution
within test vessels 12 and sample tubes 13. In a more general
sense, the present invention provides an method for reducing
carryover of and precisely delivering liquid from a source
container to a target container by spinning the target container so
that any liquid within the target container is removed from the
vicinity of the dispensing means. For the purpose of describing the
invention, reference will be made to the aforedescribed sample tube
13 as a source container and test vessel 12 as a target
container.
[0021] FIG. 2 illustrates a test vessel 12 as a target container
having an amount of liquid 14 previously disposed therein, for
example an amount of reagent taken from a compartment 23 and
dispensed therein by liquid reagent aspirating probe 25. Test
vessel 12 is shown as being generally symmetrical around axis 36
for purposes of illustration only. In practicing the present
invention, a target container need not be symmetrical as long as it
may be rotated around a central axis as described next. Prior to
the introduction into target test vessel 12 of additional liquid
taken from a source container sample tube 13 by sample aspirating
probe 28, target test vessel 12 is caused to rotate around axis 36
by a source 34 of rotational motion. Rotational source 34 may
comprise a motor shaft with a tube clamp mounted thereon, a
friction belt driven by a motor, or other similar mechanisms for
rotating target test vessel 12 around axis 36 at a speed sufficient
to cause liquid 14 disposed therein to move upwards from the bottom
40 of target test vessel 12 along the inner walls 42 and away from
the central portion 46 thereof, as illustrated in FIG. 3. By
spinning the target container 12, liquid therein is removed from
the path of a sample aspirating probe 28, as illustrated in FIG. 4,
containing an amount of sample liquid 30 aspirated therein. In the
present invention, sample aspirating probe 28 may have either of a
permanent type or of a disposable type aspirating probe design.
[0022] As a result of liquid within the target container 12 being
removed from the path of sample aspirating probe 28, aspirating
probe 28 may be inserted and lowered into the target container 12 a
sufficient distance to bring a droplet of source liquid 32 formed
at the nozzle of the aspirating probe 28 using, for example a
peristaltic vacuum pump (not shown), into contact with the bottom
40 of the target container 12, as illustrated in FIG. 5 without the
sampling pipette or the droplet touching any of the liquid 14
previously disposed therein. Physically toughing the droplet 32
with the bottom 40 of the target container 12 releases surface
tension energy so that the droplet 32 cleanly flows into the target
container 12 and not allowing any physical contact between the
aspirating probe 28 and any liquid spun against the walls 42 of the
target container 12, as seen in FIG. 6. In FIG. 6, the previous
droplet of liquid 32 formed at the nozzle 33 of aspirating probe 28
has also spun against the walls 42 of the target container 12 and
admixed with liquid 14 maintained along the inner walls 42 of the
target container 12 by the centrifugal forces generated by
rotational motion of the target container 12. This embodiment of
the present invention is thus seen to provide a simple method for
eliminating contamination of the aspirating probe 28 dispensing
means by spinning the target container 12 so that any liquid within
the target container 12 is removed away from the dispensing means
when liquid from the source container sample tube 15 is dispensed
therein by the aspirating probe 28. After this dispensing of the
initial droplet of liquid 32 into the target container 12 by
aspirating probe 28 without touching any of the liquid 14
previously disposed therein, the sample liquid remaining within
aspirating probe 28 may similarly be dispensed into subsequent
target containers 12 without the aspirating probe 28 touching any
liquids disposed therein. This may be accomplished by axially
spinning a subsequent target vessel so that target vessel liquid
contained therein is displaced away from the central portion of the
target vessel; forming another droplet of source liquid at the
nozzle of the sampling pipette and lowering the sampling pipette
into the central portion of the subsequent target vessel a distance
sufficient to cause the second droplet of source liquid to contact
the bottom of the subsequent target vessel without the sampling
pipette or the droplet touching second target vessel liquid
disposed therein. Prior to the aspirating probe 28 being used to
aspirate any additional source liquids taken from another source
container sample tube 13, the aspirating probe 28 is typically
cleaned by insertion into a conventional wash resource 26. This
embodiment of the present invention is thereby seen to provide a
simple method for eliminating carryover of liquid aspirated and
dispensed by the aspirating probe 28 between the source container
sample tube 13, the first target test vessel 12 and any
subsequently accessed target containers 12.
[0023] In an alternate embodiment, the present invention may also
be useful in overcoming uncertainties associated with dispensing of
a known volume of aspirated liquid that arise due to any portion of
the aspirated liquid remaining behind on the exterior surface of
the nozzle. This embodiment is illustrated in FIG. 7 in which a
known volume of liquid 30 is shown as aspirated into aspirating
probe 28 using, for example a precisely metered peristaltic vacuum
pump (not shown), and the aspirating probe 28 has been inserted a
distance above the bottom 40 of an empty and stationary target
vessel 12. The peristaltic vacuum pump is operated to dispense a
major portion, for example about 98%, of the known volume of liquid
30 into the stationary target vessel 12., as shown in FIG. 8,
leaving a minor droplet portion 32, in this example about 2% of
liquid 30 within the nozzle 33 of the aspirating probe 28. The
peristaltic vacuum pump is operated so that the size of the minor
portion is sufficiently small to ensure that surface tension forces
within the droplet 32 will retain the droplet 32 at the nozzle 33
of the aspirating probe 28.
[0024] As described before, target test vessel 12 is next caused to
rotate around axis 36 by a source 34 of rotational motion at a
speed sufficient to cause liquid 30 dispensed therein to move
upwards from the bottom 40 of target test vessel 12 along the inner
walls 42 and away from the central portion 46 thereof, as
illustrated in FIG. 9. After the dispensed major portion of liquid
30 into the target container 12 is moved upwards from the bottom 40
to the inner walls 42 by centrifugal forces generated by the
rotational motion of the target test vessel 12, aspirating probe 28
may be lowered into the target vessel 12 to bring minor droplet
portion 32 at the nozzle of the aspirating probe 28 into contact
with the bottom 40 of the rotating target container 12, as
illustrated in FIG. 10, thereby releasing surface tension energy so
that the droplet 32 cleanly flows into the target vessel minimizing
the amount of any aspirated liquid remaining behind on the exterior
surface of the nozzle. The minor droplet portion 32 then admixes
with the major portion of liquid 30 along the inner walls 42 of the
target vessel 12, illustrated in FIG. 11.
[0025] In this embodiment, the present invention ensures that the
total amount of liquid 30 dispensed into the target vessel 12 is
less than the total volume of liquid 30 originally aspirated into
aspirating probe 28 and, at the same time, is greater than the
major portion of the known volume of liquid 30. It should be noted
by the reader that while this alternate embodiment may be practiced
when the target vessel 12 is originally empty, as described above,
in an instance that the target vessel 12 originally contains a
liquid 14, like shown in FIG. 2, then as described in conjunction
with FIGS. 3 and 4, the target test vessel 12 may be rotated to
cause liquid 14 disposed therein to move from the bottom 40 of
target test vessel 12 along the inner walls 42 and away from the
central portion 46 thereof, as illustrated in FIG. 3 and away from
the path of the sample aspirating probe 28, as illustrated in FIG.
4.
[0026] Such an embodiment is illustrated in FIGS. 12-17 where,
beginning with FIG. 12, a target vessel 12 contains target fluid 30
therein a and a known amount of source liquid 32 has been aspirated
from a source vessel into an aspirating probe 28. The target vessel
is spun around its axis 36, FIG. 13, so that target liquid 30
contained therein is displaced away from the central portion 46 and
the bottom portion 40 (see FIGS. 2 and 3) of the target vessel
12.
[0027] Next, the sampling pipette 28 is lowered into the central
portion 46 of the target vessel 12 a distance sufficient to cause a
major portion 50 of the volume of source liquid 32 to contact the
bottom of the target vessel 12, FIG. 14, without the major portion
12 touching target liquid 30 disposed therein, so that the major
portion 50 of source liquid 32 is spun off from the sampling
pipette 28 into the target vessel 12. The target vessel 12
continues to spin so that the target liquid 30 and the major
portion 50 of source liquid 32 contained therein are displaced away
from the central portion of the target vessel, FIG. 15, and admixed
together, illustrated as mixture 51.
[0028] Subsequently, a minor droplet 52 of the remaining portion of
source liquid 32 is formed at the nozzle of the sampling pipette 28
and the sampling pipette 28 is again lowered into the central
portion 46 of the target vessel 12 a distance sufficient to cause
the remaining minor droplet portion 52 of source liquid 32 to
contact the bottom of the target vessel 12 without the remaining
minor droplet portion 52 touching liquid mixture 51 disposed
therein, FIG. 16, so that the remaining minor droplet portion 52 of
source liquid is spun off from the sampling pipette into the target
vessel 12, FIG. 17, and admixed together with mixture 51,
illustrated as mixture 53.
[0029] It is to be understood that the embodiments of the invention
disclosed herein are illustrative of the principles of the
invention and that other modifications may be employed which are
still within the scope of the invention. For example, if small
amounts of liquid are involved, rather than spinning the target
vessel to remove liquid therein from the path of the aspirating
probe, the target vessel may be inclined at an angle to remove
liquid from the bottom portion of the target vessel so that the
aspirating probe may be lowered into the target container to bring
the droplet of liquid at the nozzle of the aspirating probe into
contact with the bottom of the target container without touching
any of the liquid previously disposed therein. Accordingly, the
present invention is not limited to those embodiments precisely
shown and described in the specification but only by the following
claims.
* * * * *